Quantitative rat liver function test by galactose single point method

2008 ◽  
Vol 42 (4) ◽  
pp. 495-504 ◽  
Author(s):  
T H Young ◽  
H S Tang ◽  
Y C Chao ◽  
H S Lee ◽  
C H Hsiong ◽  
...  

Summary The purpose of this study was to investigate the galactose single point (GSP) method, a residual liver function test recently recommended by the US Food and Drug Administration, which can be a useful tool for rat liver function measurement. Rats were treated either with carbon tetrachloride (CCl4) alone (1 mL/kg, intraperitoneally [i.p.]) for one day or with isoniazid (INH) alone (150 mg/kg, i.p.) or (in order to ameliorate the effects of INH) with a combination of INH and bis- p-nitrophenyl phosphate (BNPP) (25 mg/kg, i.p.) for 21 days. Hepatotoxicity was assayed by plasma aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activities and scores of histological activity index-necroinflammation (HAI-NI) of the respective liver specimens. The GSP method in rats was defined by the galactose blood level after 60 min. Significant differences in GSP values were observed between controls and the CCl4-treated rats. After 21 days of treatment, no significant changes in AST and ALT values were observed among the control, INH and INH-BNPP groups. There were significant differences in average GSP values for controls ( P < 0.001) and INH-BNPP ( P < 0.001) compared with INH alone. Highly significant correlations ( P < 0.001) were obtained between GSP and scores of HAI-NI for all the groups. GSP was concluded to be a more sensitive biomarker of INH-induced hepatotoxicity than AST or ALT in the rats. The GSP method has been proved to be a simple and useful tool for the quantitative determination of liver function in rats, which can possibly be extended to other animals.

RADIOISOTOPES ◽  
1973 ◽  
Vol 22 (8) ◽  
pp. 422-427
Author(s):  
Akiko KUBODERA ◽  
Susumu TSURUFUJI

2003 ◽  
Vol 124 (4) ◽  
pp. A754-A755
Author(s):  
Elwyn Elias ◽  
Charles Mills ◽  
Marc Halphen ◽  
Norman Barras ◽  
Hans-Juergen Gruss

1928 ◽  
Vol 25 (8) ◽  
pp. 675-677
Author(s):  
A. R. Bernheim

1967 ◽  
Vol 2 (22) ◽  
pp. 974-976 ◽  
Author(s):  
N. McK. Bennett ◽  
J. A. Forbes ◽  
C. R. Lucas ◽  
A. Kucers

2010 ◽  
Vol 138 (5) ◽  
pp. S-482
Author(s):  
Janet Fallon ◽  
Manish Thakker ◽  
Tim J. Parke ◽  
Neil Rajoriya

1980 ◽  
Vol 14 (10) ◽  
pp. 702-709 ◽  
Author(s):  
Cal Wayne Greenlaw

A number of complications associated with total parenteral nutrition (TPN) have been identified, and methods of prevention or treatment have been developed. However, abnormal liver function continues to occur with the use of TPN, and little is known about its incidence and etiology. Twenty-three patients, receiving TPN through the TPN program at Holy Cross Hospital from January, 1978 to May, 1978, were studied. All patients received a basic parenteral amino acid solution (Travasol®), with varying amounts of nitrogen per day, depending on nitrogen balance studies. Dextrose was supplied in quantities necessary to provide 120 percent or more of the patient's calculated basal energy expenditure (BEE). Of the 23 patients studied, elevated liver function test values were detected in two patients (8.6 percent). In both cases, the complication developed within six to eight days, and both had received calories in excess of 213 percent of their calculated BEE and had a calorie to nitrogen (kcal: N) ratio greater than 150: 1. Mean calories as a percent of calculated BEE and kcal: N ratio were significantly higher in the patients with elevated liver function test (LFT) values than in those with normal LFT values ( p < 0.05 and p < 0.005, respectively). Following identification of the elevated LFT values, both patients were immediately placed on cyclic TPN (CyTPN). In the one patient, liver enzymes reverted toward normal after seven days of CyTPN, while the second patient required only five days. Cyclic TPN was deemed effective in the reversal of abnormal liver function in these two patients. It is speculated that the abnormal liver function was a result of fatty liver infiltration. The mechanism by which this infiltration occurs and its treatment are discussed.


Sign in / Sign up

Export Citation Format

Share Document